Total synthesis of malagashanine: a chloroquine potentiating indole alkaloid with unusual stereochemistry

The first total synthesis of malagashanine, a chloroquine potentiating indole alkaloid, is presented. A highly stereoselective cascade annulation reaction was developed to generate the tetracyclic core of the Malagasy alkaloids. This chemistry is likely to be broadly applicable to the synthesis of o...

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Veröffentlicht in:Chemical science (Cambridge) 2017-01, Vol.8 (1), p.697-700
Hauptverfasser: Kong, A, Mancheno, D E, Boudet, N, Delgado, R, Andreansky, E S, Blakey, S B
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Sprache:eng
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Zusammenfassung:The first total synthesis of malagashanine, a chloroquine potentiating indole alkaloid, is presented. A highly stereoselective cascade annulation reaction was developed to generate the tetracyclic core of the Malagasy alkaloids. This chemistry is likely to be broadly applicable to the synthesis of other members of this stereochemically unique family of natural products.
ISSN:2041-6520
2041-6539
DOI:10.1039/c6sc03578g